NDC 24623-042 Advanced Lightning
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24623 - Cbi Laboratories, Inc
- 24623-042 - Advanced Lightning
Product Packages
NDC Code 24623-042-22
Package Description: 56.7 g in 1 JAR
Product Details
What is NDC 24623-042?
What are the uses for Advanced Lightning?
Which are Advanced Lightning UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Advanced Lightning Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- SODIUM SULFITE (UNII: VTK01UQK3G)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- CUCUMBER (UNII: YY7C30VXJT)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".